A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7526



Internal ID15552544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:101156925..101190052hg38UCSC Ensembl
Outerchr10:102916682..102949809hg19UCSC Ensembl
Outerchr10:102906672..102939799hg18UCSC Ensembl
Outerchr10:102906672..102939799hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg386312
hg196312
hg186312
hg176312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8837
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7526
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer